Compositions

ABSTRACT

A surfactant composition comprising: 
     (a) a surfactant material; 
     (c) a polyethylene imine of the general formula —(CH 2 CH 2 NH) n —; and 
     (d) an aromatic, monoethylenically-unsaturated carboxylic acid ester of the formula 
     
       
         
         
             
             
         
       
     
     where R 1  is selected from the group consisting of hydrogen, C 1 -C 16  alkyl, C 1 -C 16  alkoxy, aryl and substituted aryl, and R 2  is selected from the group consisting of aryl, substituted aryl and C 6 -C 16  alkyl; the materials (b)-(d) each having an odour value of 10,000 maximum. 
     The problem of rancidity, commonly encountered when low-grade surfactant materials are used, especially in soaps, is considerably reduced.

This invention relates to surfactant compositions, especially those forwashing and treating substrates and to methods of preventing undesirableodours as a result of their use.

In this description, the use of the term “surfactant composition” meansany composition comprising materials having affinity for both aqueousand non-aqueous phases when used in conjunction with water in a cleaningapplication, including the washing and conditioning of substrates. Thesematerials can be the synthetic surfactants (anionic, cationic andnon-ionic) widely used, and also the more traditional materials such assaponified animal and vegetable fats. Examples include washingdetergents, fabric conditioners, and soaps of all kinds.

In this description, the use of the term “substrates” means any surfacethat may require washing or conditioning and includes fabric, textile,skin, hair, glass, ceramic etc.

In many parts of the world, surfactant compositions use low quality rawmaterials, which have an unpleasant odour and which can impart thisunpleasant odour to the substrate being treated. In particular, bars ofsoap used for washing clothing, textiles, skin, hair, cooking utensils,and dishes, are often made from relatively cheap materials, typicallymaterials derived from animal and vegetable fats. A problem universallyencountered with such products is malodor. This is provoked by variousfactors, such as heat, humidity and presence of other additives, and itmay develop and become worse over time. This can be overcome by theaddition of perfume to counteract the malodour, but this solution is notonly expensive but also not always effective.

It has now been found that this problem may be substantially or evencompletely overcome by the use of a particular formulation, in that themalodour can be counteracted and even a pleasant odour can be imparted,without the need for a perfume addition. The invention thereforeprovides a surfactant composition comprising:

-   -   (a) a surfactant material;    -   (b) a polyethylene imine of the general formula        —(CH₂CH₂NH)_(n)—; and    -   (c) an aromatic, monoethylenically-unsaturated carboxylic acid        ester of the formula

where R¹ is selected from the group consisting of hydrogen, C₁-C₁₆alkyl, C₁-C₁₆ alkoxy, aryl and substituted aryl, and R² is selected fromthe group consisting of aryl, substituted aryl and C₆-C₁₆ alkyl; thematerials (b) and (c) each having an odour value of 10,000 maximum.

The use of the singular in the definition shown above also includes theplural.

The parameter of Odour Value (hereinafter “OV”) is well known to theart. It is determined by the method of Neuner and Etzweiler, and isdescribed in the standard reference work “Perfumes: Art, Science andTechnology” (Elsevier, 1991) at p. 153. Preferably the materials (b) and(c) have an OV of less than 5,000, more preferably less than 2,000 andmost preferably less than 1000.

Polyethylene imines are materials composed of ethylene imine units—CH₂CH₂NH—. The chains may be branched, in which case the hydrogen onthe nitrogen is replaced by another chain of ethylene imine units.Polyethylene imines are water-soluble and are used in a variety ofcommercial applications. Examples of commercially-available polyethyleneimines useful in this invention include the range sold under the tradename LUPASOL (ex BASF). These are available in various grades, withmolecular weights from 800 to 2 mio. Da. The same OVs as for aldehydesapply to the polyethylene imines.

The esters of the formula hereinabove depicted may be any such esters.Preferably R¹ is hydrogen, C₁₋₈ alkyl, C₁-₈ alkoxy or aryl, andindependently of this, R² is preferably C₆-₁₂ alkyl or aryl.

By “surfactant material” is meant any substance or combination ofsubstances that are useful for cleansing and conditioning substrates,when used in conjunction with water. This definition comprehends notonly the surfactant blends used in laundry and dishwashing detergentsand softening and conditioning agents, but also the more traditionalsoap raw materials, such as saponified natural oils. This invention maybe used in conjunction with any of these, but it is especially usefulwith low-grade soap materials of the type often used in laundry barsoaps in parts of Asia and Latin America. Such materials areparticularly prone to malodour over time and the use of this inventionconsiderably reduces this, and may even eliminate it completely.

The surfactant compositions of this invention may also use any of theknown materials used by the art in wash and treatment compositions, inart-recognised quantities. One preferred such material is solvent; it ispreferred that the materials (b) and (c) are first dissolved in solventprior to their addition to the surfactant material, as this makes theirincorporation easier. Typical solvents include dipropylene glycol,diethyl phthalate, isopropyl myristate and benzyl benzoate.

In an especially preferred embodiment of the invention, the compositionsadditionally include a fragrant aldehyde, whose OHV has a value of10,000 maximum, preferably less than 5,000, more preferably less than2,000 and most preferably less than 1000.

A list of aldehydes, suitable for use in this invention, is shown below;this list is exemplary only and other aldehydes not shown here are alsosuitable for use in the invention.

Another known material that may be used is fragrance. Although thisinvention can eliminate completely malodour and even itself impart apleasing odour, it may be desirable to impart a particular fragrance tothe composition. This may be done by using one or more of the manyfragrances known to the art, in art-recognised quantities. One of theadvantages of this invention is that, with the reduction or eliminationof malodour, less perfume (an expensive component) is necessary toachieve a desired effect. The fragrances are generally solutions inorganic solvent, and they may be added to the mixture of materials (b)and (c) and solvent hereinabove mentioned.

Other art-recognised ingredients, such as builders, buffers, fillers,antistatic agents, fungicides, antioxidants, dyes, pigments, fluorescingagents, bactericides and skin emollients, may also be used inart-recognised quantities.

The compositions of the invention are prepared by mixing the ingredientsin the known manner. As hereinabove described, it is preferred to mixmaterials (b) and (c) first, with aldehyde, when required, preferablywith solvent, and then mix this mixture into material (a), to give acomposition according to the invention. The proportions should be suchthat

-   -   (i) when no fragrant aldehyde is present, the composition will        contain a minimum concentration by weight of each of (b) and (c)        of from 0.005-0.5%.    -   (ii) when at least one fragrant aldehyde is present, (b) and (c)        are each present in the composition to the extent of from        0.005%-10%.

Preferably

-   -   (iii) when fragrance is present, materials (b)+(c), +aldehyde,        where present, are each present to the extent of from 0.001-5.0%        by weight of materials (a)+(b)+(c)+aldehyde; and    -   (iv) when no fragrance is present, materials (b)+(c), +aldehyde,        where present, are each present to the extent of from 0.01-2.0%        by weight of materials (a)+(b)+(c)+aldehyde.

By substantially or even completely overcoming the problem of rancidityfrequently encountered with low-grade laundry materials, the inventionallows their use in a much wider range of applications. The inventiontherefore provides a composition for the reduction of rancidity inlaundry materials prone thereto, the composition comprising:

-   -   (a) a polyethylene imine of the general formula        —(CH₂CH₂NH)_(n)—; and    -   (b) an aromatic, monoethylenically-unsaturated carboxylic acid        ester of the formula

where R¹ is selected from the group consisting of hydrogen, C₁-C₁₆alkyl, C₁-C₁₆ alkoxy, aryl and substituted aryl, and R² is selected fromthe group consisting of aryl, substituted aryl and C₆-C₁₆ alkyl; thematerials (b) and (c) each having an odour value of 10,000 maximum.

Preferably the composition additionally contains fragrant aldehyde, ashereinabove described.

The invention further provides a method of reducing rancidity in alaundry material prone thereto, comprising the addition thereto of acomposition consisting essentially of

-   -   (a) a polyethylene imine of the general formula        —(CH₂CH₂NH)_(n)—; and    -   (b) an aromatic, monoethylenically-unsaturated carboxylic acid        ester of the formula

where R¹ is selected from the group consisting of hydrogen, C₁-C₁₆alkyl, C₁-C₁₆ alkoxy, aryl and substituted aryl, and R² is selected fromthe group consisting of aryl, substituted aryl and C₆-C₁₆ alkyl; thematerials (b)-(d) each having an odour value of 10,000 maximum.

Preferably there is also added fragrant aldehyde, as hereinabovedescribed.

The invention is now further described with reference to the followingnon-limiting examples. In these examples, combinations of materials (b)and (c), and fragrant aldehyde were tested in different soap bases inthe absence (examples 1-3) and in the presence (examples 4-6) ofperfume.

EXAMPLE 1

A mixture of 5% (wt) dihydrofarnesal(3,7,11-trimethyl-dodeca-6,10-dienal) (component (b)), 20% LUPASOL™ G100 (50% active level, viscosity 1200 mPa-s, molecular weight(weight-average) 5000 (component (c)), 15% octyl methoxy cinnamate(component (d)), and 60% isopropyl myristate (60%) was prepared andadded at a dosage of 0.2% by weight to soap bases as hereinunderdescribed. The base was milled thoroughly and soap cakes made. The cakeswere allowed to macerate for one day and evaluated olfactively. Soapcakes were made without the mixture and used as comparisons.

Evaluation was carried out on the strength of the fragrance note and howwell the fragrance covered the base note. Various soap bases with strongto mild inherent base odours were evaluated by a panel and were given arating as below:

Perfume Strength Base Odour Coverage Very Strong 5 Excellent CoverageStrong 4 Very Good Coverage Good 3 Good Coverage Moderate 2 WeakCoverage Weak 1 Base Odour Noticeable Base Odour Rating without withmixture mixture Soap Base 1 1.9 4.0 Soap Base 2 2.0 4.1 Soap Base 3 2.14.1 Soap Base 4 1.9 4.0

Soap Base 1 was 100% soap base (usually contains about 15-20% water) ofplant origin (usually referred to as 80/20, meaning made from 80% palmoil and 20% coconut oil).

Soap Base 2 was a mixture of soap base (90% Soap Base 1)+10% talc (thistype of combination is usually used in making premium toilet soaps).

Soap Base 3 was a mixture of soap base (80% Soap Base 1)+20% talc (thistype of combination is usually used in making mid-price toilet soaps).

Soap Base 4 was a mixture of soap base (60% Soap Base 1)+40% talc (thistype of combination is usually used in making low-cost toilet soaps).

EXAMPLE 2

A mixture of 10% dihydrofarnesal, 10% LUPASOL SK (25% active content,viscosity 500-1000 mPa-s and molecular weight 2,000,000), 5% geranylcrotanate and 75% dipropylene glycol was prepared and added at a dosageof 0.3% into soap bases of the types shown 5 below. The base was milledthoroughly and soap cakes made. Soap cakes without the mixture were alsomade. The cakes were allowed to macerate for one day and evaluatedolfactively as described in Example 1.

Base Odour Rating without with mixture mixture Soap Base 5 1.8 4.6 SoapBase 6 2.1 4.5 Soap Base 7 1.9 4.6 Soap Base 8 1.9 4.6

Soap Base 5 was 100% soap base (usually contains about 15-20% water) ofplant origin, prepared from a mixture of crude palm oil and palm fattyacid distillate.

Soap Base 6 was a mixture of soap base (90% Soap Base 5)+10% talc (thistype of combination is usually used in making premium toilet soaps).

Soap Base 7 was a mixture of soap base (80% Soap Base 5)+20% talc (thistype of combination is usually used in making mid-price toilet soaps).

Soap Base 8 was a mixture of soap base (60% Soap Base 5)+40% talc (thistype of combination is usually used in making low-cost toilet soaps).

EXAMPLE 3

A mixture of 10% dihydrofarnesal, 20% LUPASOL™ G 35 (50% active level,viscosity=450 mPa-s, average MW 2000), 20% dihexyl fumarate and 50%diethyl phthalate was prepared and added at a dosage of 0.1% into soapbases as described below and soap cakes made. Soap cakes without themixture were also made. The cakes were allowed to macerate for one dayand evaluated olfactively.

Base Odour Rating without with mixture mixture Soap Base 9 1.9 4.0 SoapBase 10 2.0 4.1 Soap base 11 2.1 4.1 Soap base 12 1.9 4.0

Soap Base 9 was 100% soap base (usually contains about 15-20% water) oftallow origin.

Soap Base 10 was a mixture of soap base (90% Soap Base 9)+10% talc (thistype of combination is usually used in making premium toilet soaps).

Soap Base 11 was a mixture of soap base (80% Soap Base 9)+20% talc (thistype of combination is usually used in making mid-price toilet soaps).

Soap Base 12 was a mixture of soap base (60% Soap Base 9)+40% talc (thistype of combination is usually used in making low-cost toilet soaps).

EXAMPLE 4

A mixture of 5% dihydrofarnesal, 10% LUPASOL™ HF (50% active content,viscosity 14,000 mPa-s and molecular weight 50,000), 5% geranylcrotanate and 80% dipropylene glycol was prepared and mixed with aperfume (perfume 80%+mixture 20%). This mixture was dosed at 1.5% intosoap bases as described hereinunder. The base was milled thoroughly andsoap cakes made. The cakes were allowed to macerate for one day andevaluated olfactively. Control soap cakes (without the mixture andcontaining only the perfume at 1.5% dosage) were also made and tested.

Base Odour Coverage Perfume Strength Rating Rating without with withoutwith mixture mixture mixture mixture Soap Base A 4.2 4.8 2.1 4.7 SoapBase B 4.1 4.9 1.9 4.5 Soap Base C 4.1 4.9 1.9 4.8 Soap Base D 4.0 4.82.0 4.8

Perfume dosage in the soap base was 1.5% and the perfume contained 30%solvent. In the case of soaps to which the mixture was added, theproportion of solvent was reduced by the quantity of mixture present.

Soap Base A was made from 100% soap base (usually contains about 15-20%water) of plant origin (usually referred to as 80/20, meaning made from80% palm oil and 20% coconut oil)

Soap Base B was made from a mixture of soap base (90% Soap Base 1)+10%talc (this type of combination is usually used in making premium toiletsoaps)

Soap Base C was made from a mixture of soap base (80% Soap Base 1)+20%talc (this type of combination is usually used in making mid-pricetoilet soaps).

Soap Base D was made from a mixture of soap base (60% Soap Base 1)+40%talc (this type of combination is usually used in making low-cost toiletsoaps).

EXAMPLE 5

A mixture of 15% dihydrofarnesal, 5% LUPASOL™ PS (33% active content,viscosity 1400 mPa-s and MW 750,000), 5% LUPASOL™ G 100 (50% activelevel, viscosity 1200 mPa-s, and average MW 5000), 5% octyl methoxycinnamate, and 70% isopropyl myristate was prepared and mixed with aperfume (perfume 90%+mixture 10%). This mixture was dosed at 1.2% intosoap bases as described hereinunder. The base was milled thoroughly andsoap cakes made. The cakes were allowed to macerate for one day andevaluated olfactively. Control soap cakes (without the mixture andcontaining only perfume at 1.2% dosage) were also prepared and tested.

Base Odour Coverage Perfume Strength Rating Rating without with withoutwith mixture mixture mixture mixture Soap Base E 4.2 4.7 1.6 4.5 SoapBase F 4.0 4.9 1.9 4.6 Soap Base G 3.9 4.8 1.7 4.8 Soap Base H 3.6 4.92.0 4.8

Soap Base E was made from 100% soap base (usually contains about 15-20%water) of plant origin prepared from a mixture of crude palm oil andpalm fatty acid distillate.

Soap Base F was made from a mixture of soap base (90% Soap Base 5)+10%talc (this type of combination is usually used in making premium toiletsoaps).

Soap Base G was made from a mixture of soap base (80% Soap Base 5)+20%talc (this type of combination is usually used in making mid-pricetoilet soaps).

Soap Base H was made from a mixture of soap base (60% Soap Base 5)+40%talc (this type of combination is usually used in making low-cost toiletsoaps).

EXAMPLE 6

A mixture of 5% dihydrofarnesal, 10% LUPASOL™ G 100 (50% active level,viscosity 1200 mPa-s, average MW 5000), 25% octyl methoxy cinnamate and60% benzoyl benzoate was prepared and mixed with a perfume (perfume 85%+mixture 15%). This mixture was dosed at 1.6% into soap bases asdescribed hereinunder. The base was milled thoroughly and soap cakesmade. The cakes were allowed to macerate for one day and evaluatedolfactively. Control soap cakes (without the mixture and containing onlyperfume at 1.6% dosage) were also made and tested.

Base Odour Coverage Perfume Strength Rating Rating without with withoutwith mixture mixture mixture mixture Soap Base J 4.5 4.9 2.1 4.5 SoapBase K 4.6 4.9 1.9 4.6 Soap Base L 4.4 4.8 1.8 4.8 Soap Base M 4.6 4.92.0 4.8

Soap Base J was 100% soap base (usually contains about 15-20% water) oftallow origin,

Soap Base K was made from a mixture of soap base (90% Soap Base 9)+10%talc (this type of combination is usually used in making premium toiletsoaps).

Soap Base L was made from a mixture of soap base (80% Soap Base 9)+20%talc (this type of combination is usually used in making mid-pricetoilet soaps).

Soap Base M was made from a mixture of soap base (60% Soap Base 9)+40%talc (this type of combination is usually used in making low-cost toiletsoaps).

EXAMPLE 7

A translucent personal wash soap base that had a fatty malodor had thefollowing respective ingredients in the table below mixed in and themass was milled, extruded and stamped in the form of a bar. One litre ofheadspace off the bar was taken at a rate of 100 ml a minute for 10minutes and analyzed by gas chromatography and mass spectrometry.

The malodor components were identified and their level quantified. Thecolor of the bars were assessed a 5 point scale by where 1=no coloration5=strong brown color. The results were:

% Headspace Reduction Coloration Control  0 1 soap base plus 0.1%LUPASOL ™ FG 61 2 soap base plus 0.2% LUPASOL FG 66 4 soap base plus 0.2DHF 32 1 soap base plus 0.10% LUPASOL + 70 3 0.10% DHF soap base plus0.05% + 0.15% DHF 83 2 soap base plus 0.05% + 0.135% DHF + 76 2 0.015%GC Where DHF = dihexyl fumarate and GC = geranyl crotonate

LUPASOL™ FG alone provides a significant reduction in the malodor of thesoap base. However the soap is an unacceptable yellow brown color. Thebenefit of LUPASOL can be improved and the color minimized to anacceptable level by using it in combination with dihexyl fumarate or amixture of dihexyl fumarate and geranyl crotonate

EXAMPLE 8

The soap base of Example 7 had added thereto 1% of a commercial soapfragrance added, alone or with the combination of materials below.Samples were prepared and analysed as above.

% Headspace Reduction Coloration soap base plus 1% fragrance-Control 212 soap base plus 1% fragrance + 0.2% 87 4 LUPASOL ™ FG soap base plus 1%fragrance + 0.05% 89 2 LUPASOL FG + 0.15 DHF soap base plus 1%fragrance + 0.10% 91 3 LUPASOL FG + 0.10 DHF

LUPASOL alone significantly reduces the malodor in the presence of afragrance; however, the color is unacceptable. In combination withdihexyl fumarate an acceptable color can be achieved and excellent thegood malodor reduction obtained.

1. (canceled)
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 5. (canceled) 6.(canceled)
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 8. A method of reducing rancidity in asurfactant material prone thereto, comprising the addition thereto of acomposition consisting essentially of a polyethylene imine of thegeneral formula —(CH₂CH₂NH)_(n)— wherein n has value such that thepolyethylene imine has a molecular weight of from 800 to 2 mio. Da.; ;and an aromatic, mono ethylenically-unsaturated carboxylic acid ester ofthe formula

where R¹ is selected from the group consisting of hydrogen, C₁-C₁₆alkyl, C₁-C₁₆ alkoxy, aryl and substituted aryl, and R² is selected fromthe group consisting of aryl, substituted aryl and C₆-C₁₆ alkyl; andoptionally, a fragrant aldehyde, the polyethylene imine, the aromatic,monoethylenically-unsaturated carboxylic acid ester and, when present,the fragrant aldehyde, each having an Odour Value of 10,000 maximum. 9.A method according to claim 8, in which R¹ is selected from hydrogen,C₁₋₈ alkyl, C₁₋₈ alkoxy and aryl.
 10. A method according to claim 8, inwhich R² is selected from C₆-₁₂ alkyl and aryl.
 11. A method accordingto claim 8, in which the fragrant aldehyde has an odour value of lessthan 5,000.
 12. A method according to claim 8, in which: (i) when atleast one fragrant aldehyde is present, the polyethylene imine, thearomatic, monoethylenically-unsaturated carboxylic acid ester are eachpresent in the composition to the extent of from 0.005%-10%; and (ii)when no (d) fragrant aldehyde is present, the composition contains from0.005-0.5% of each of polyethylene imine, the aromatic,monoethylenically-unsaturated carboxylic acid ester.
 13. A methodaccording to claim 8, in which the fragrant aldehyde is selected fromthe group consisting of the following compounds:


14. A method according to claim 8, wherein the method comprises thefurther step of: adding the composition to one or more laundry materialsto reduce the rancidity thereof.